Assessing regulatory variant effect scores by massively... - Martin Kircher - VarI - ISMB/ECCB 2017
Decoding Transcriptional Regulation by Genome-Wide Reporter Assays and Large-Scale Transfection
Introduction to Deep Mutational Scanning (Animation)
Manolis Kellis on Dissecting Disease Circuitry at Single-Cell Resolution
A Systematic Strategy to Link Human Genetic Variations to Drug Response | Divya Kriti
What is Copy number variation (CNV)? Copy number variation analysis in genome. Importance.
Next Generation Sequencing - A Step-By-Step Guide to DNA Sequencing.
Kipoi Seminar - Dmitry Penzar (MSU)
VarI SIG - Correlates of... - Martin Kircher - Special Interest Groups (SIGs) - ISMB/ECCB 2015
Overcoming sequence artifacts to fuel clinically relevant NGS applications
Weida Tong - The FDA’s experience with emerging genomics technologies – past, present and future
SVS Sequence Analysis Module Demonstration
The Center for Genomic Interpretation's ELEVATEGenetics service. (CGI ELEVATE Genetics 2019/2020)
How to Select the Best Genetic Test in Nephrology | Clear & Complete Overview
ESHG14 Poster: Whole Transcriptome Analysis of Testicular Germ Cell Tumors
20180409 5 SIFT Polyphen quantitation
TCGA Project Update - Brad Ozenberger
Tina Lockwood - Clinical next generation sequencing for precision cancer therapeutics
Sequencing for Cancer Risk with Sandra Balladares
Robert Brown Thesis Defense
